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Volumn 62, Issue 21, 1997, Pages 7234-7238

Theoretical Study of Strong Basicity in Aromatic Diamines

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EID: 0000494543     PISSN: 00223263     EISSN: None     Source Type: Journal    
DOI: 10.1021/jo970689z     Document Type: Article
Times cited : (22)

References (38)
  • 24
    • 85033144892 scopus 로고    scopus 로고
    • note
    • Another pair of orbitals consists mainly of diffuse atomic functions in each of the fragments, the proton and an amine, and gives a negligibly small overlap population.
  • 27
    • 0001425104 scopus 로고
    • 3, respectively, in an isolated state. This indicates that the differences in the basic strength are traced back to these amines in an isolated state, as has already been noticed by Howard et al. See: Howard, S. T.; Foreman, J. P.; Edwards, P. G. Can. J. Chem. 1997, 75, 60.
    • (1994) J. Phys. Chem. , vol.98 , pp. 1436
    • Fujimoto, H.1    Satoh, S.2
  • 28
    • 0030818961 scopus 로고    scopus 로고
    • 3, respectively, in an isolated state. This indicates that the differences in the basic strength are traced back to these amines in an isolated state, as has already been noticed by Howard et al. See: Howard, S. T.; Foreman, J. P.; Edwards, P. G. Can. J. Chem. 1997, 75, 60.
    • (1997) Can. J. Chem. , vol.75 , pp. 60
    • Howard, S.T.1    Foreman, J.P.2    Edwards, P.G.3
  • 35
    • 84961978628 scopus 로고    scopus 로고
    • The MP2//RHF/6-31G* calculations of monoprotonated species of diamines fail to give barriers for proton transfer. See, for a detailed analysis: Peräkylä, M. J. Org. Chem. 1996, 61, 7420.
    • (1996) J. Org. Chem. , vol.61 , pp. 7420
    • Peräkylä, M.1
  • 38
    • 1542687299 scopus 로고
    • Foresman, J. B.; Frisch, M. J. Exploring Chemistry with Electronic Structure Methods; Gaussian, Inc.: Pittsburgh, PA, 1995; p 114. See also: Yamabe, S.; Hirao, K.; Wasada, H. J. Phys. Chem. 1992, 96, 10261.
    • (1992) J. Phys. Chem. , vol.96 , pp. 10261
    • Yamabe, S.1    Hirao, K.2    Wasada, H.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.